azithromycin dihydrate
Generic: azithromycin dihydrate
Labeler: direct rxDrug Facts
Product Profile
Brand Name
azithromycin dihydrate
Generic Name
azithromycin dihydrate
Labeler
direct rx
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
azithromycin dihydrate 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-090
Product ID
72189-090_2be8149b-0d04-e882-e063-6394a90a5b86
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208249
Listing Expiration
2026-12-31
Marketing Start
2020-05-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189090
Hyphenated Format
72189-090
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
azithromycin dihydrate (source: ndc)
Generic Name
azithromycin dihydrate (source: ndc)
Application Number
ANDA208249 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 2 TABLET, FILM COATED in 1 BOX (72189-090-02)
- 3 TABLET, FILM COATED in 1 BOX (72189-090-03)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2be8149b-0d04-e882-e063-6394a90a5b86", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656", "749780"], "spl_set_id": ["a6426d5f-5518-3c69-e053-2995a90af50f"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOX (72189-090-02)", "package_ndc": "72189-090-02", "marketing_start_date": "20200522"}, {"sample": false, "description": "3 TABLET, FILM COATED in 1 BOX (72189-090-03)", "package_ndc": "72189-090-03", "marketing_start_date": "20200522"}], "brand_name": "AZITHROMYCIN DIHYDRATE", "product_id": "72189-090_2be8149b-0d04-e882-e063-6394a90a5b86", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "72189-090", "generic_name": "AZITHROMYCIN DIHYDRATE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AZITHROMYCIN DIHYDRATE", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA208249", "marketing_category": "ANDA", "marketing_start_date": "20200522", "listing_expiration_date": "20261231"}